EP0140020A1 - Multi-purpose on column injector - Google Patents

Multi-purpose on column injector Download PDF

Info

Publication number
EP0140020A1
EP0140020A1 EP84110322A EP84110322A EP0140020A1 EP 0140020 A1 EP0140020 A1 EP 0140020A1 EP 84110322 A EP84110322 A EP 84110322A EP 84110322 A EP84110322 A EP 84110322A EP 0140020 A1 EP0140020 A1 EP 0140020A1
Authority
EP
European Patent Office
Prior art keywords
injector
duct
sample
column
tube
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP84110322A
Other languages
German (de)
French (fr)
Other versions
EP0140020B1 (en
Inventor
Fausto Munari
Giovanni Ostan
Carlo Saravalle
Bruno Tosi
Sorin Trestianu
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fisons Instruments SpA
Original Assignee
Carlo Erba Strumentazione SpA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from IT2287583U external-priority patent/IT8322875V0/en
Priority claimed from IT2243284U external-priority patent/IT8422432V0/en
Application filed by Carlo Erba Strumentazione SpA filed Critical Carlo Erba Strumentazione SpA
Priority to AT84110322T priority Critical patent/ATE39186T1/en
Publication of EP0140020A1 publication Critical patent/EP0140020A1/en
Application granted granted Critical
Publication of EP0140020B1 publication Critical patent/EP0140020B1/en
Expired legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/04Preparation or injection of sample to be analysed
    • G01N30/16Injection
    • G01N30/18Injection using a septum or microsyringe
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/04Preparation or injection of sample to be analysed
    • G01N30/06Preparation
    • G01N30/12Preparation by evaporation
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/04Preparation or injection of sample to be analysed
    • G01N30/16Injection
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/04Preparation or injection of sample to be analysed
    • G01N30/06Preparation
    • G01N30/12Preparation by evaporation
    • G01N2030/126Preparation by evaporation evaporating sample
    • G01N2030/127PTV evaporation
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/04Preparation or injection of sample to be analysed
    • G01N30/06Preparation
    • G01N30/10Preparation using a splitter

Definitions

  • This invention relates to an injector for the injection of samples to be analyzed in a gas chromatographic capillary column and,.more precisely, to an injector of the non vaporizing direct on-column type, comprising an accessory device applicable thereof to allow its use also to perform injections of the vaporizing type with not dilutable samples or concentrated solutions requiring a splitting of the vaporized sample, as well as to eliminate the solvent before the sample is transferred to the capillary column.
  • Said injector comprises a duct for the introduction of the injection syringe needle which can be closed by means of a valve, the lower section of said duct housing the end of a gas chromatographic column.
  • Said gas chromatographic column end is pneumatically connected to the duct thanks to an 0-ring kept in position by a small tube coaxial to the column and screwed to the injector body.
  • This small tube forms a jacket around the column head and the hollow space between the jacket and the column is fed with a fluid at a controlled temperature.
  • the vaporization tube can be void or a fiberglass sponge can be placed in it to hold the sample when it is at the liquid state and to release it when it passes to the vapour state.
  • the fiberglass sponge is impermeable to the sample at the liquid state, while it is permeable to the sample when the letter is at the vapour state.
  • An object of this invention is now to provide an injector of the non-vaporizing direct on-column type, for instance such as the one described and illustrated in the aforementioned U.S. patent N. 4.269.608 and comprising an accessory device which allows to use said injector to perform a method of the type described and claimed in the aforementioned U.S. patent N. 4.383.839.
  • Another object of the present invention is to provide an injector with accessory device having the abovementioned features, which is capable of holding inside the vaporization tube the sample at the liquid state and of releasing it when it passes to the vapour state, even in the case of very polar samples, for which the use of said fiberglass sponges could involve drawbacks due to their high surface and the difficulty of completely desactivating them.
  • Another object of this invention is to provide an injector with an accessory device of the aforementioned type,which allows to eliminate, during the injection stage and in any case before the vaporization stage, the volatile components present in a sample to be analyzed, thus allowing to analyze only the heavy components in the sample itself.
  • an on-column type injector with accessory device which comprises a tubular element, one end of which can be fixed to the injector body coaxially to the duct for the passage of the injection syringe needle, while the opposite accessory device end is closed by an insert provided with an axial hole, in which the head of a capillary gas chromatographic column is pneumatically housed, and with a hole for controllaby splitting the vaporized sample, the tubular element housing a vaporization tube in conditions of thermal exchange with heating means and pneumatically connected to said passage for the injection syringe needle and to said holes of the insert.
  • the vaporization tube can have a series of inner protrusions,turned towards the axis of the tube itself and reciprocally offset and opposed in such a way as to hold the sample when it is at the liquid state.
  • the end of said tubular element in which the gas chromatographic column head in inserted can have, besides the hole necessary to perform the vaporized sample splitting, a second hole communicating with a duct connected, through a valve, to a carrier gas line.
  • Said duct can moreover be connected, downstreams of said valve and by means of a fitting provided with an adjustable neck, to the duct for the introduction of the sample carrier gas, while the valve can be a three-way valve, allowing a selective connection of the car- ri e r gas line to the duct for carrier gas introduction into the on-column injector or to the duct leading to the tubular element.
  • the aforementioned second hole in the tubular element during the injection of the sample to be analyzed and in any case before the vaporization stage of the sample portion to be trasferred to the capillary column, it is possible to introduce carrier gas into the tubular element through said second hole and in such a way to strike the sample with a gas current flowing in the opposite direction to that of the sample introduction in the gas chromatographic column, said gas current carrying the sample volatile substances out of the on-column injector by means of a suitable discharge duct provided in the injector body and equipped with cut off and control valves.
  • the lower part of the injector shows a protrusion 3 coaxial to the duct 2 allowing the injector to be fixed to the walls 4 of an oven which houses a gas chromatographic capillary column 5, in particular preferably made of fused silica.
  • the protrusion 3 has a threaded cavity 6 coaxial to the duct 2 and in which said duct 2 and a duct 6' open, the latter duct communicating with a fluid source at controlled temperature, for example, even if not exclusively, air, possibly controlled by a valve 6".
  • a small tube coaxial to the initial part of the column is screwed in the threaded cavity 6, forming a collecting chamber for the fluid at controlled temperature coming from the duct 6'.
  • an accessory device 8 formed by a tubular element 7 is screwed instead of said small tube; in the lower end of said tubular element 7 is screwed an insert 9 provided with two radial holes 10 and 10' and with an axial hole 11, wherein the gas chromatographic column head 5 is inserted and pneumatically sealed and mechanically locked by a gasket 9' and a locking nut 9".
  • a vaporization tube 12 is positioned, the upper end of which is inserted in the duct 2 of the injector and pneumatically sealed by means of an 0-ring 13 pressed against the injector body by the tubular element itself.
  • the lower end of tube 12 is inserted in the axial hole 11 of insert 9 and pneumatically sealed by means of a gasket 14.
  • the lower end of tubular element 7 has a threaded cavity 21 provided with a shoulder 22 capable of holding a washer 23 made of insulating material, for instance Vespel (registered trade mark), against which the gasket 14 is pushed by the insert 9.
  • the first of the two radial holes 10 and 10' of insert 9 communicates with a duct 10" and is designed to allow splitting of the vaporized sample, while the second hole 10 1 communicates with a duct 10" connected, through a three-way valve 29 to which the duct 1 is also connected, to a source of carrier gas.
  • the ducts 1' and 10"' can be connected to one another, downstream the valve 29, by a duct 30 provided with an adjustable neck 31.
  • the inner part of the vaporization tube 12 can house a fiberglass sponge, or it can be provided, in an intermediate section between a point A downstream the injection point and a point B upstream the open end of column 5, with a series of protrusions 20 turned towards the axis of the tube itself and reciprocally offset and opposed, in a way as to create a zigzag passage for the injected sample.
  • the protrusion 20 hold inside the tube 12 the sample when it is at the liquid state so as to prevent it from penetrating into the gaschromatographic column before it is vaporized.
  • tubular element 7 Between the inner side walls of tubular element 7 and the vaporization tube 12 there is an hollow space 15 communicating through one or more holes 16, with said cavity 6 and therefore with duct 6' leading to the cavity itself and, through one or more holes 17, with the oven chamber, in a way as to submit the vaporization tube 12 to the controlled thermal action of the fluid introduced in 6' and discharged in 17.
  • Said fluid is generally intended for cooling the tube 12, but it is also possible to introduce hot fluid for sample vaporization.
  • an electric resistor 18 wound around the tube 12 and having an end soldered to a small metal cylinder 24, soldered on its turn in the upper axial passage of element 7.
  • the other end of resistor 18 is soldered to a small metal cylinder 25 fixed between the ring 23 and a shaped insulating gasket 27, while the other electrode 28 is grounded in a point whatever.
  • the injector body 1 has a third duct 32 for discharge, which is inserted in the duct 2 upstream the vaporization tube 12 and has a first valve 32' for controlling the discharge flow rate and a second valve 32" to control the duct opening and closure.
  • the tubular element 7 is fixed to the injector 1 and the gas chromatographic column head is connected, through insert 9, to the vaporization tube 12, in particular it is inserted with its free end straight into the lower part of the vaporization tube 12.
  • Figures 2 and 3 show another embodiment of the invention, wherein the vaporization tube 12 is housed in a tubular element 40 in a material adapted for heat transfer,for instance in a metallic material.
  • This tubular element is heated by a plurality of resistors 44 housed in tubular insulating sheats 42.
  • a liner 46 made of aluminium, or any other direct or indirect heating means can be provided for.
  • the valve (not illustrated) to open and close duct 2 of the injector is opened and the upper part of the vaporization tube 12 receives through the duct 2 the injection syringe needle containing a sample to be analyzed which is at the liquid state.
  • the sample is injected into the tube 12, the syringe needle is removed and the valve controlling the duct 12, is closed.
  • the fiberglass sponge inserted in the tube 12 or the protrusions 20 on the tube wall prevent the sample at the liquid state from penetrating into the column 5.
  • the temperature of tube 12 is kept at such a value as to prevent sample vaporization by means of cooling fluid introduced in 6' and discharged in 17.
  • the tube 12 may be heatedto a controlled temperature to eliminate by the back flush or splitting line well defined light sample component not interesting the analysis.
  • the vaporization tube 12 is heated at a chosen temperature for instance by the electric resistor 18, until the sample is completely vaporized.
  • the carrier gas which flows into the injector duct,2, coming from duct 1, enters the vaporization tube 20 and drags the vaporized sample towards the chromatographic column. Part of the mixture formed by the vaporized sample and the carrier gas can be deviated outside the column 5 and discharged through the duct 10 of insert 9 so that the column receives only a certain amount of vaporized sample.
  • the ratio between the amount of mixture deviated by the duct 10 is determined by controlling the flow rate in said duct and the opening or closing of same through the control valve 33 and cut off valve 33' connected to the duct 10, according to the temperature of tube 12.
  • a splitless injection can be made by closing valve 33'.
  • a cooling gas for example ambient air
  • Said gas after lapping the tube 12, flows into the oven chamber through holes 17 provided in the lower part of the tubular element.
  • the duct 10"' is fed with inert gas. More detail ediy when the syringe needle to inject the sample has been introduced into the duct 2, the valve 29 is regulated in such a way that only the duct 10"' communicates with the inert gas source, the valve 31 is regulated in such a way that the duct 10"' is connected to the duct 1' while the valve 32" of the discharge duct is open.
  • the carrier gas sent to the duct 10"' comes out from the hole 10' of the insert 9, partly penetrating into the gas chromatographic column and partly into the tube 12.
  • a small fraction of carrier gas introduced in the duct 10"' passes through the duct 30 and the neck 31 and flows into the duct 1.
  • the sample is injected into the tube 12 where it meets the opposite inert gas current coming in through the duct 10"'; in this way the more volatile substances present in the sample are dragged by the carrier gas towards the opposite direction to that of sample introduction into the gas chromatographic column and sent out of the injector through duct 32 and under the control of valve 32', for example a needle valve.
  • valve 32' for example a needle valve.
  • the heaviest part of the sample is held by the protrusions 20 of tube 12 when striked by the carrier gas flow coming from hole 10' of insert 9 and dragging the sample volatile substances.
  • the valve 29 is regulated in such a way that the carrier gas flows only into the duct 1' and the valve 32" of the discharge duct is closed.
  • the duct 10"' is kept in communication with duct 1' so that a fraction of carrier gas flowing to the duct 1' comes out from the radial hole 10' of the insert 9 preventing the vaporized sample from entering the duct 10"'.
  • the adjustable neck 31 is designed to control the gas flow rate necessary to create a fluid cap, alternatively in the duct 1' during the stage of elimination of the volatile substances present in the sample, and in the radial hole 10' during the vaporization stage and the sample injection in the gas chromatographic column.

Abstract

The invention relates to a direct on-column non vaporizing injector for gas chromatographic analyses and comprising an accessory device capable of allowing injection with sample vaporization and possible splitting. The accessory device is formed by a tubular element which, at one end, can be fixed to the injector body, coaxially to the passage for the injection syringe needle, while its opposite end is closed by an insert provided with an axial hole in which the gas chromatographic capillary column head is pneumatically inserted, and with at least one hole for splitting the vaporized sample. The tubular element houses a vaporization tube which is in conditions of thermal exchange with heating means is pneumatically connected to said passage for the injection syringe needle and to said insert holes and receives the upper end of the gas chromatographic column.

Description

  • This invention relates to an injector for the injection of samples to be analyzed in a gas chromatographic capillary column and,.more precisely, to an injector of the non vaporizing direct on-column type, comprising an accessory device applicable thereof to allow its use also to perform injections of the vaporizing type with not dilutable samples or concentrated solutions requiring a splitting of the vaporized sample, as well as to eliminate the solvent before the sample is transferred to the capillary column.
  • From U.S. Patent No. 4.269.608 assigned to the same Assegnee it is known an injector to perform the injection of samples to be analyzed without vaporization, directly in the gas chromatographic column.
  • Said injector comprises a duct for the introduction of the injection syringe needle which can be closed by means of a valve, the lower section of said duct housing the end of a gas chromatographic column.
  • Said gas chromatographic column end is pneumatically connected to the duct thanks to an 0-ring kept in position by a small tube coaxial to the column and screwed to the injector body. This small tube, according to what described and claimed in the aforementioned patent, forms a jacket around the column head and the hollow space between the jacket and the column is fed with a fluid at a controlled temperature.
  • From U.S. Patent No. 4.383839 it is also known a method for the injection with vaporization of a liquid sample in a gas chromatographic capillary column comprising the steps of
    • a) injecting the liquid sample into the initial part of a sample vaporization tube which does not contain stationary liquid phase (or contains an immobilised phase), the sample being kept liquid during the whole injection process;
    • b) heating the vaporization tube and feeding it with carrier gas to drag the vaporized sample;
    • c) diverting part of the resulting mixture of vaporized sample and carrier gas by means of a splitter and sending the remaining part to a gas chromatographic column containing a stationary liquid phase for chromatographic separation.
  • The vaporization tube can be void or a fiberglass sponge can be placed in it to hold the sample when it is at the liquid state and to release it when it passes to the vapour state. In fact, the fiberglass sponge is impermeable to the sample at the liquid state, while it is permeable to the sample when the letter is at the vapour state.
  • An object of this invention is now to provide an injector of the non-vaporizing direct on-column type, for instance such as the one described and illustrated in the aforementioned U.S. patent N. 4.269.608 and comprising an accessory device which allows to use said injector to perform a method of the type described and claimed in the aforementioned U.S. patent N. 4.383.839.
  • Another object of the present invention is to provide an injector with accessory device having the abovementioned features, which is capable of holding inside the vaporization tube the sample at the liquid state and of releasing it when it passes to the vapour state, even in the case of very polar samples, for which the use of said fiberglass sponges could involve drawbacks due to their high surface and the difficulty of completely desactivating them.
  • Another object of this invention is to provide an injector with an accessory device of the aforementioned type,which allows to eliminate, during the injection stage and in any case before the vaporization stage, the volatile components present in a sample to be analyzed, thus allowing to analyze only the heavy components in the sample itself.
  • Said objects are achieved by an on-column type injector with accessory device which comprises a tubular element, one end of which can be fixed to the injector body coaxially to the duct for the passage of the injection syringe needle, while the opposite accessory device end is closed by an insert provided with an axial hole, in which the head of a capillary gas chromatographic column is pneumatically housed, and with a hole for controllaby splitting the vaporized sample, the tubular element housing a vaporization tube in conditions of thermal exchange with heating means and pneumatically connected to said passage for the injection syringe needle and to said holes of the insert.
  • In particular, the vaporization tube can have a series of inner protrusions,turned towards the axis of the tube itself and reciprocally offset and opposed in such a way as to hold the sample when it is at the liquid state.
  • Moreover, the end of said tubular element in which the gas chromatographic column head in inserted, can have, besides the hole necessary to perform the vaporized sample splitting, a second hole communicating with a duct connected, through a valve, to a carrier gas line. Said duct can moreover be connected, downstreams of said valve and by means of a fitting provided with an adjustable neck, to the duct for the introduction of the sample carrier gas, while the valve can be a three-way valve, allowing a selective connection of the car- rier gas line to the duct for carrier gas introduction into the on-column injector or to the duct leading to the tubular element.
  • Thanks to the aforementioned second hole in the tubular element, during the injection of the sample to be analyzed and in any case before the vaporization stage of the sample portion to be trasferred to the capillary column, it is possible to introduce carrier gas into the tubular element through said second hole and in such a way to strike the sample with a gas current flowing in the opposite direction to that of the sample introduction in the gas chromatographic column, said gas current carrying the sample volatile substances out of the on-column injector by means of a suitable discharge duct provided in the injector body and equipped with cut off and control valves.
  • The invention will be now described more in detail with reference to the attached drawings.
    • Fig. 1 is a cross-sectional view of an on-column injector equipped with a vaporization accessory device and provided with a system for the elimination of the volatile components present in the sample to be analyzed.
    • Fig. 2 is a cross-sectional view of a modified embodiment of the vaporization accessory device according to the invention.
    • Fig. 3 is a section taken along the line III-III of fig.2.
  • Referring to figure 1, the injector 1, for example such as the one described and illustrated in the aforementioned U.S. Patent No. 4.269.608 comprises a duct 2, which can be closed by a valve, capable of allowing the passage of the injection syringe needle, and a duct 1' for the introduction of carrier gas. The lower part of the injector shows a protrusion 3 coaxial to the duct 2 allowing the injector to be fixed to the walls 4 of an oven which houses a gas chromatographic capillary column 5, in particular preferably made of fused silica.
  • The protrusion 3 has a threaded cavity 6 coaxial to the duct 2 and in which said duct 2 and a duct 6' open, the latter duct communicating with a fluid source at controlled temperature, for example, even if not exclusively, air, possibly controlled by a valve 6".
  • In the known embodiment, a small tube coaxial to the initial part of the column is screwed in the threaded cavity 6, forming a collecting chamber for the fluid at controlled temperature coming from the duct 6'.
  • According to the invention, in said threaded cavity 6, an accessory device 8 formed by a tubular element 7 is screwed instead of said small tube; in the lower end of said tubular element 7 is screwed an insert 9 provided with two radial holes 10 and 10' and with an axial hole 11, wherein the gas chromatographic column head 5 is inserted and pneumatically sealed and mechanically locked by a gasket 9' and a locking nut 9".
  • Inside the tubular element 7, a vaporization tube 12 is positioned, the upper end of which is inserted in the duct 2 of the injector and pneumatically sealed by means of an 0-ring 13 pressed against the injector body by the tubular element itself. The lower end of tube 12 is inserted in the axial hole 11 of insert 9 and pneumatically sealed by means of a gasket 14. In particular, the lower end of tubular element 7 has a threaded cavity 21 provided with a shoulder 22 capable of holding a washer 23 made of insulating material, for instance Vespel (registered trade mark), against which the gasket 14 is pushed by the insert 9.
  • The first of the two radial holes 10 and 10' of insert 9 communicates with a duct 10" and is designed to allow splitting of the vaporized sample, while the second hole 101 communicates with a duct 10" connected, through a three-way valve 29 to which the duct 1 is also connected, to a source of carrier gas. Moreover, the ducts 1' and 10"' can be connected to one another, downstream the valve 29, by a duct 30 provided with an adjustable neck 31.
  • The inner part of the vaporization tube 12 can house a fiberglass sponge, or it can be provided, in an intermediate section between a point A downstream the injection point and a point B upstream the open end of column 5, with a series of protrusions 20 turned towards the axis of the tube itself and reciprocally offset and opposed, in a way as to create a zigzag passage for the injected sample. The protrusion 20 hold inside the tube 12 the sample when it is at the liquid state so as to prevent it from penetrating into the gaschromatographic column before it is vaporized.
  • Between the inner side walls of tubular element 7 and the vaporization tube 12 there is an hollow space 15 communicating through one or more holes 16, with said cavity 6 and therefore with duct 6' leading to the cavity itself and, through one or more holes 17, with the oven chamber, in a way as to submit the vaporization tube 12 to the controlled thermal action of the fluid introduced in 6' and discharged in 17. Said fluid is generally intended for cooling the tube 12, but it is also possible to introduce hot fluid for sample vaporization. However, for the latter purpose, it is more advisable, as illustrated, to use an electric resistor 18, wound around the tube 12 and having an end soldered to a small metal cylinder 24, soldered on its turn in the upper axial passage of element 7.The other end of resistor 18 is soldered to a small metal cylinder 25 fixed between the ring 23 and a shaped insulating gasket 27, while the other electrode 28 is grounded in a point whatever.
  • Finally the injector body 1 has a third duct 32 for discharge, which is inserted in the duct 2 upstream the vaporization tube 12 and has a first valve 32' for controlling the discharge flow rate and a second valve 32" to control the duct opening and closure.
  • The tubular element 7 is fixed to the injector 1 and the gas chromatographic column head is connected, through insert 9, to the vaporization tube 12, in particular it is inserted with its free end straight into the lower part of the vaporization tube 12.
  • Figures 2 and 3 show another embodiment of the invention, wherein the vaporization tube 12 is housed in a tubular element 40 in a material adapted for heat transfer,for instance in a metallic material. This tubular element is heated by a plurality of resistors 44 housed in tubular insulating sheats 42. To heat the splitting point, which is a very important feature, a liner 46 made of aluminium, or any other direct or indirect heating means can be provided for.
  • To perform an injection with or without elimination of the volatile components(back-flush), the following operations must be accomplished.
  • The valve (not illustrated) to open and close duct 2 of the injector is opened and the upper part of the vaporization tube 12 receives through the duct 2 the injection syringe needle containing a sample to be analized which is at the liquid state.
  • The sample is injected into the tube 12, the syringe needle is removed and the valve controlling the duct 12, is closed. The fiberglass sponge inserted in the tube 12 or the protrusions 20 on the tube wall prevent the sample at the liquid state from penetrating into the column 5. On the other hand, during injection the temperature of tube 12 is kept at such a value as to prevent sample vaporization by means of cooling fluid introduced in 6' and discharged in 17. If required, the tube 12 may be heatedto a controlled temperature to eliminate by the back flush or splitting line well defined light sample component not interesting the analysis.
  • At this point, after eventual interruption or commutation of cooling, the vaporization tube 12 is heated at a chosen temperature for instance by the electric resistor 18, until the sample is completely vaporized. The carrier gas which flows into the injector duct,2, coming from duct 1, enters the vaporization tube 20 and drags the vaporized sample towards the chromatographic column. Part of the mixture formed by the vaporized sample and the carrier gas can be deviated outside the column 5 and discharged through the duct 10 of insert 9 so that the column receives only a certain amount of vaporized sample. In particular, the ratio between the amount of mixture deviated by the duct 10 (splitting ratio) is determined by controlling the flow rate in said duct and the opening or closing of same through the control valve 33 and cut off valve 33' connected to the duct 10, according to the temperature of tube 12. Of course, a splitless injection can be made by closing valve 33'.
  • At the end of the analysis, in order to rapidly cool the tube 12, a cooling gas, for example ambient air, is introduced through the injector duct 7, into the hollow space 15 of the tubular element. Said gas, after lapping the tube 12, flows into the oven chamber through holes 17 provided in the lower part of the tubular element.
  • In case the sample to be analyzed contains volatile substances which must not enter the gas chromatographic column, during the sample injection stage and before the sample vaporization, the duct 10"' is fed with inert gas. More detail ediy when the syringe needle to inject the sample has been introduced into the duct 2, the valve 29 is regulated in such a way that only the duct 10"' communicates with the inert gas source, the valve 31 is regulated in such a way that the duct 10"' is connected to the duct 1' while the valve 32" of the discharge duct is open. The carrier gas sent to the duct 10"' comes out from the hole 10' of the insert 9, partly penetrating into the gas chromatographic column and partly into the tube 12.
  • A small fraction of carrier gas introduced in the duct 10"' passes through the duct 30 and the neck 31 and flows into the duct 1. At this point the sample is injected into the tube 12 where it meets the opposite inert gas current coming in through the duct 10"'; in this way the more volatile substances present in the sample are dragged by the carrier gas towards the opposite direction to that of sample introduction into the gas chromatographic column and sent out of the injector through duct 32 and under the control of valve 32', for example a needle valve. The small fraction of inert gas coming out from the duct 1' prevents the volatile substances from entering the duct 1' itself.
  • The heaviest part of the sample is held by the protrusions 20 of tube 12 when striked by the carrier gas flow coming from hole 10' of insert 9 and dragging the sample volatile substances. When this stage of elimination of the more volatile substances present in the sample is over and the sample vaporization stage begins, the valve 29 is regulated in such a way that the carrier gas flows only into the duct 1' and the valve 32" of the discharge duct is closed. The duct 10"' is kept in communication with duct 1' so that a fraction of carrier gas flowing to the duct 1' comes out from the radial hole 10' of the insert 9 preventing the vaporized sample from entering the duct 10"'.
  • The adjustable neck 31 is designed to control the gas flow rate necessary to create a fluid cap, alternatively in the duct 1' during the stage of elimination of the volatile substances present in the sample, and in the radial hole 10' during the vaporization stage and the sample injection in the gas chromatographic column.

Claims (11)

1. A direct on column non vaporizing injector for gaschromatographic analyzers, comprising an accessory device for vaporization injections, in the form of a tubular element which: can be fixed, at one end, to the injector body, coaxially to an injector passage for the injection syringe needle, while the opposite element end is closed by an insert provided with an axial hole where the head of a gas chromatographic capillary column is inserted and pneumatically sealed, and with at least one hole for the vaporized sample splitting, said tubular element housing a vaporization tube which is in conditions of thermal exchange with heating means, is connected to said injector passage for the injection syringe needle and to said insert holes, and receives the upper end of the gas chromatographic column.
2. An injector according to claim 1, wherein at least the zone of said insert near said splitting hole is directly or indirectly heated.
3. An injector according to claim 1, wherein said heating means consists of an electric resistor wound around the vaporization tube and fed by electrodes.
4. An injector according to claim 1, wherein said heating means comprise means for heating said accessory device tubular member.
5. An injector according to claim 1, wherein said vaporization tube has an inner section having a series of protrusions turned towards the axis of the tube itself and reciprocally offset and opposed so as to hold the injected sample when it is at the liquid state.
6. An injector according to claim 1, wherein between the internal side walls of said tubular element and the vaporization tube a hollow space is provided which pneumatically communicates at one end with an injector duct connected to a source of fluid at a controlled temperature and, at the opposite end, with the oven chamber to which the injector is fixed.
7. An injector according to claim 6, wherein the upper end of said tubular element is shaped in such a way as to match with the cavity of the injector body, instead of a small tube, coaxial to the column and forming the collecting chamber for the cooling fluid which is usually present in said direct non vaporizing injector.
8. An injector according to claim 1, wherein the end of said tubular element in which the gas chromatographic column head is inserted presents, besides said hole for the vapcri- zed sample splitting, a second hole communicating with a first duct connected, through a valve, to a source of carrier gas.
9. An injector according to claim 8, wherein said first duct is connected, downstream said valve and by means of a second duct provided with an adjustable neck, to a third duct for the introduction of carrier gas into the on-column injector.
10. An injector according to claims 8 and 9, wherein the injector body hasy between the upper end of the vaporization tube and said third duct for the introduction of carrier gas, a fourth discharge duct leading to the passage for the syringe needle and controlled by a valve system.
11. An injector according to claim 10, wherein valve system includes a needle valve controlling the discharge flow rate and a cut off valve.
EP84110322A 1983-09-09 1984-08-30 Multi-purpose on column injector Expired EP0140020B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT84110322T ATE39186T1 (en) 1983-09-09 1984-08-30 MULTIPURPOSE DIRECT INPUT IN COLUMNS.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
IT2287583U 1983-09-09
IT2287583U IT8322875V0 (en) 1983-09-09 1983-09-09 ACCESSORY FOR GAS CHROME INJECTORS.
IT2243284U 1984-06-29
IT2243284U IT8422432V0 (en) 1984-06-29 1984-06-29 REFINEMENTS FOR GAS CHROMATOGRAPHIC INJECTORS.

Publications (2)

Publication Number Publication Date
EP0140020A1 true EP0140020A1 (en) 1985-05-08
EP0140020B1 EP0140020B1 (en) 1988-12-07

Family

ID=26328194

Family Applications (1)

Application Number Title Priority Date Filing Date
EP84110322A Expired EP0140020B1 (en) 1983-09-09 1984-08-30 Multi-purpose on column injector

Country Status (3)

Country Link
US (1) US4559063A (en)
EP (1) EP0140020B1 (en)
DE (1) DE3475569D1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU596709B2 (en) * 1987-11-03 1990-05-10 Vsesojuzny Nauchno-Issledovatelsky I Konstruktorsky Institut Khromatografii Method of chromatographic analysis of a mixture of liquid substances and a gas chromatograph for carrying out the method
EP0451566A2 (en) * 1990-04-07 1991-10-16 Eberhard Gerstel Process and device for gas-chromatographic separation
CN108051532A (en) * 2017-12-06 2018-05-18 安徽皖仪科技股份有限公司 Separate sealed injection port

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1184320B (en) * 1985-02-21 1987-10-28 Erba Strumentazione PROCEDURE AND DEVICE FOR DIRECT INJECTION INTO COLUMNS OF SAMPLES CONTAINING HIGH BOILING AND / OR MEDIOVOLATILE COMPOUNDS
US5032151A (en) * 1990-01-17 1991-07-16 Hewlett-Packard Company System and method for automated cool on-column injection with column diameters less than 530 μm
US5083450A (en) * 1990-05-18 1992-01-28 Martin Marietta Energy Systems, Inc. Gas chromatograph-mass spectrometer (gc/ms) system for quantitative analysis of reactive chemical compounds
IT1247522B (en) * 1991-04-24 1994-12-17 Erba Strumentazione GAS CHROMATOGRAPHIC INJECTOR
US5228514A (en) * 1992-11-19 1993-07-20 Ruska Laboratories, Inc. Gas trap apparatus
US5686656A (en) * 1996-02-27 1997-11-11 Aviv Amirav Method and device for the introduction of a sample into a gas chromatograph
US6203597B1 (en) * 1998-04-15 2001-03-20 G. L. Scince, Inc. Method and apparatus for mass injection of sample
DE19817016C2 (en) * 1998-04-17 2000-02-03 Gerstel Gmbh & Co Kg Sample application device for a gas chromatograph
US5997615A (en) * 1998-06-23 1999-12-07 Luong; Huan V. Large-sample accessory for a gas chromatograph
GB9904225D0 (en) * 1999-02-25 1999-04-21 Egmond W M A Injection liner with integral profiling such that it can be fitted with an injection septum and cap
NL1012127C2 (en) 1999-05-21 2000-11-23 Sgt Exploitatie Bv Assembly for desorbing sampling tubes, as well as an adapter and sampling tubes apparently intended for such an assembly, as well as a kit of parts for forming such an assembly.
US6494939B1 (en) * 1999-09-16 2002-12-17 Perkinelmer Instruments Llc Zero-dilution split injector liner gas chromatography
IT1313986B1 (en) * 1999-10-29 2002-09-26 Thermoquest Italia Spa STEAM INJECTOR
US6719826B2 (en) * 2002-07-15 2004-04-13 Saika Technological Institute Foundation Method and apparatus for sample injecting in gas chromatography
US7384457B2 (en) * 2005-10-21 2008-06-10 Agilent Technologies, Inc. Seal for gas chromatography
US8522600B2 (en) 2010-10-12 2013-09-03 Saudi Arabian Oil Company Fluid compositional analysis by combined gas chromatographic and direct flash methods

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1174540B (en) * 1961-08-29 1964-07-23 Balansen En Gewichtenfabriek J Sampler for liquids
US3401565A (en) * 1966-02-28 1968-09-17 Armour & Co Liquid sampling apparatus for gas chromatography
DE2755566A1 (en) * 1977-12-13 1979-06-21 Hewlett Packard Gmbh Glass capillary gas chromatograph splitter - integral with displacement tube sealed against evaporator tube
GB2030055A (en) * 1978-09-26 1980-04-02 Erba Strumentazione Sample injection into gas chromatorgraphic columns
GB2039777A (en) * 1979-01-17 1980-08-20 Erba Strumentazione Vaporization Injector for Gas Chromatographic Columns
EP0051778A2 (en) * 1980-11-06 1982-05-19 CARLO ERBA STRUMENTAZIONE S.p.A. A device for vaporization injection in a gas-chromatographic column

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3063286A (en) * 1959-07-14 1962-11-13 Standard Oil Co Sample introduction system for gas chromatography apparatus
US3230046A (en) * 1962-10-29 1966-01-18 Beroza Morton Apparatus and method for ultramicro determination of the carbon skeleton and other structural features of organic compounds
US3244152A (en) * 1964-03-10 1966-04-05 Beckman Instruments Inc Sample vaporizer
US3401552A (en) * 1966-01-17 1968-09-17 Maryon W. Ruchelman Automatic sample injector
US3463012A (en) * 1966-09-29 1969-08-26 Hamilton Co Probe sampling apparatus
US3592046A (en) * 1969-02-27 1971-07-13 Hamilton Co Precolumn inlet for chromatographs
US4035168A (en) * 1974-07-24 1977-07-12 The Regents Of The University Of California Nonreactive inlet splitter for gas chromatography and method
SU1041925A1 (en) * 1979-08-16 1983-09-15 Специальное Конструкторское Бюро Газовой Хроматографии Gas chromatograph
US4422860A (en) * 1982-01-26 1983-12-27 Varian Associates, Inc. On-column capillary gas chromatographic injector

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1174540B (en) * 1961-08-29 1964-07-23 Balansen En Gewichtenfabriek J Sampler for liquids
US3401565A (en) * 1966-02-28 1968-09-17 Armour & Co Liquid sampling apparatus for gas chromatography
DE2755566A1 (en) * 1977-12-13 1979-06-21 Hewlett Packard Gmbh Glass capillary gas chromatograph splitter - integral with displacement tube sealed against evaporator tube
GB2030055A (en) * 1978-09-26 1980-04-02 Erba Strumentazione Sample injection into gas chromatorgraphic columns
GB2039777A (en) * 1979-01-17 1980-08-20 Erba Strumentazione Vaporization Injector for Gas Chromatographic Columns
EP0051778A2 (en) * 1980-11-06 1982-05-19 CARLO ERBA STRUMENTAZIONE S.p.A. A device for vaporization injection in a gas-chromatographic column

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
JOURNAL OF CHROMATOGRAPHY, vol. 151, 1978, pages 311-320, Elsevier Scientific Publishing Company, Amsterdam, NL; K. GROB et al.: "On-column injection on to glass capillary columns" *
JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY & CHROMATOGRAPHY COMMUNICATIONS, vol. 2, no. 6, June 1979, pages 366-370; M. GALLI et al.: "Special cooling system for the on-column injector in capillary gas chromatography eliminating discrimination of sample compounds" *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU596709B2 (en) * 1987-11-03 1990-05-10 Vsesojuzny Nauchno-Issledovatelsky I Konstruktorsky Institut Khromatografii Method of chromatographic analysis of a mixture of liquid substances and a gas chromatograph for carrying out the method
EP0451566A2 (en) * 1990-04-07 1991-10-16 Eberhard Gerstel Process and device for gas-chromatographic separation
EP0451566A3 (en) * 1990-04-07 1992-11-25 Eberhard Gerstel Process and device for gas-chromatographic separation
CN108051532A (en) * 2017-12-06 2018-05-18 安徽皖仪科技股份有限公司 Separate sealed injection port

Also Published As

Publication number Publication date
EP0140020B1 (en) 1988-12-07
DE3475569D1 (en) 1989-01-12
US4559063A (en) 1985-12-17

Similar Documents

Publication Publication Date Title
EP0140020A1 (en) Multi-purpose on column injector
EP0051778B1 (en) A device for vaporization injection in a gas-chromatographic column
US4300393A (en) Sample introduction apparatus for gas chromatographic analysis using packed or capillary bore open tubular columns and method of testing
US4766760A (en) Method of chromatographic analysis of a mixture of liquid substances and a gas chromatograph for carrying out the method
US4124358A (en) Sample-injection device for process gas chromatography with capillary columns
DE19653406C1 (en) Gas chromatographic sample feeding method
US5672810A (en) Gas chromatograph apparatus for a liquid sample containing a solvent
US5759234A (en) Method and device for the injection of liquid samples in a gas chromatograph
US4004881A (en) Apparatus for generating carrier gas-test specimen vapor mixtures for delivery into a gas chromatograph
US6203597B1 (en) Method and apparatus for mass injection of sample
US4442217A (en) Sample injection
EP2394158B1 (en) Apparatus and method for preparing samples for gas chromatography
EP0753739B1 (en) Process and device for the injection of large volumes of liquid samples in a gaschromatograph
WO2006077912A1 (en) Method of analysis with gas chromatograph through large-amount injection thereinto and apparatus therefor
EP0699303B1 (en) Process and device for gas chromatographic analysis of large volume samples
GB2039777A (en) Vaporization Injector for Gas Chromatographic Columns
JPS62192657A (en) Thermal cracking device with standard sample introducing device
JP3367293B2 (en) Gas chromatograph sample introduction method
JPS61194356A (en) Direct non-vaporization on-column injection method and device
JPS6078347A (en) On-column injector
SU1741061A1 (en) Capillary gas chromatograph
EP0513086B1 (en) Gas chromatography method and apparatus
JPH09311128A (en) Gas-phase component analyzing apparatus
JP3541558B2 (en) Gas chromatograph sample introduction device
JPH1114613A (en) Gas chromatograph device

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): AT BE CH DE FR GB LI NL SE

17P Request for examination filed

Effective date: 19851024

17Q First examination report despatched

Effective date: 19870129

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE FR GB LI NL SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19881207

Ref country code: LI

Effective date: 19881207

Ref country code: CH

Effective date: 19881207

Ref country code: BE

Effective date: 19881207

Ref country code: AT

Effective date: 19881207

REF Corresponds to:

Ref document number: 39186

Country of ref document: AT

Date of ref document: 19881215

Kind code of ref document: T

REF Corresponds to:

Ref document number: 3475569

Country of ref document: DE

Date of ref document: 19890112

ET Fr: translation filed
REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19900723

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19900829

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19900831

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19910830

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19920301

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee
GBPC Gb: european patent ceased through non-payment of renewal fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19920430

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19930930

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19950503